calculate_eigenvectors_wecare_only_jan2017
started: Alexey Larionov, 2016
last updated: Alexey Larionov, 09Feb2017
Summary
Overall, eigenvectors are calculated for 3 datasets:
- wecare-only (all variants and common variants)
- wecare-nfe (all variants and common variants)
- wecare-nfe-50kgen (overlapped-variants and overlapped-common-variants)
This script deals with wecare-only dataset. Additionally it exports data to text files to repeat wecare-only calculations in eigenstrat.
start_section
# Time stamp
Sys.time()## [1] "2017-02-09 16:04:39 GMT"# Folders
setwd("/scratch/medgen/scripts/wecare_stat_01.17/scripts")
interim_data_folder <- "/scratch/medgen/scripts/wecare_stat_01.17/interim_data"
# Required libraries
library(dplyr)##
## Attaching package: 'dplyr'## The following objects are masked from 'package:stats':
##
## filter, lag## The following objects are masked from 'package:base':
##
## intersect, setdiff, setequal, unionlibrary(ggplot2)
library(plotly)##
## Attaching package: 'plotly'## The following object is masked from 'package:ggplot2':
##
## last_plot## The following object is masked from 'package:stats':
##
## filter## The following object is masked from 'package:graphics':
##
## layoutload_data
load(paste(interim_data_folder, "r04_filter_cases_jan2017.RData", sep="/"))check_data
ls()## [1] "interim_data_folder" "wecare_nfe_exac.df"
## [3] "wecare_nfe_genotypes.mx" "wecare_nfe_kgen.df"
## [5] "wecare_nfe_phenotypes.df" "wecare_nfe_variants.df"dim(wecare_nfe_genotypes.mx)## [1] 275516 678class(wecare_nfe_genotypes.mx)## [1] "matrix"wecare_nfe_genotypes.mx[1:5,1:5]## HG00097 HG00099 HG00100 HG00102 HG00106
## Var000000002 0 0 NA NA 0
## Var000000008 0 NA 0 0 0
## Var000000009 0 0 0 0 0
## Var000000012 0 0 NA 0 0
## Var000000013 0 0 NA 0 0dim(wecare_nfe_phenotypes.df)## [1] 678 28str(wecare_nfe_phenotypes.df)## 'data.frame': 678 obs. of 28 variables:
## $ wes_id : chr "HG00097" "HG00099" "HG00100" "HG00102" ...
## $ gwas_id : chr NA NA NA NA ...
## $ merged_id : chr NA NA NA NA ...
## $ filter : chr "pass" "pass" "pass" "pass" ...
## $ cc : num -1 -1 -1 -1 -1 -1 -1 -1 -1 -1 ...
## $ setno : int NA NA NA NA NA NA NA NA NA NA ...
## $ family_history: int NA NA NA NA NA NA NA NA NA NA ...
## $ age_dx : int NA NA NA NA NA NA NA NA NA NA ...
## $ age_ref : num NA NA NA NA NA NA NA NA NA NA ...
## $ rstime : num NA NA NA NA NA NA NA NA NA NA ...
## $ eig1_gwas : num NA NA NA NA NA NA NA NA NA NA ...
## $ eig2_gwas : num NA NA NA NA NA NA NA NA NA NA ...
## $ eig3_gwas : num NA NA NA NA NA NA NA NA NA NA ...
## $ stage : num NA NA NA NA NA NA NA NA NA NA ...
## $ er : num NA NA NA NA NA NA NA NA NA NA ...
## $ pr : num NA NA NA NA NA NA NA NA NA NA ...
## $ hist_cat : chr NA NA NA NA ...
## $ hormone : num NA NA NA NA NA NA NA NA NA NA ...
## $ chemo_cat : chr NA NA NA NA ...
## $ br_xray : int NA NA NA NA NA NA NA NA NA NA ...
## $ br_xray_dose : num NA NA NA NA NA NA NA NA NA NA ...
## $ age_menarche : num NA NA NA NA NA NA NA NA NA NA ...
## $ age_1st_ftp : num NA NA NA NA NA NA NA NA NA NA ...
## $ age_menopause : num NA NA NA NA NA NA NA NA NA NA ...
## $ num_preg : num NA NA NA NA NA NA NA NA NA NA ...
## $ bmi_age18 : num NA NA NA NA NA NA NA NA NA NA ...
## $ bmi_dx : num NA NA NA NA NA NA NA NA NA NA ...
## $ bmi_ref : num NA NA NA NA NA NA NA NA NA NA ...wecare_nfe_phenotypes.df[1:5,1:5]## wes_id gwas_id merged_id filter cc
## HG00097 HG00097 <NA> <NA> pass -1
## HG00099 HG00099 <NA> <NA> pass -1
## HG00100 HG00100 <NA> <NA> pass -1
## HG00102 HG00102 <NA> <NA> pass -1
## HG00106 HG00106 <NA> <NA> pass -1dim(wecare_nfe_variants.df)## [1] 275516 23colnames(wecare_nfe_variants.df)## [1] "SplitVarID" "SYMBOL" "TYPE"
## [4] "CHROM" "POS" "REF"
## [7] "ALT" "AC" "AF"
## [10] "AN" "Consequence" "SIFT_call"
## [13] "SIFT_score" "PolyPhen_call" "PolyPhen_score"
## [16] "CLIN_SIG" "cDNA_position" "CDS_position"
## [19] "Codons" "Protein_position" "Amino_acids"
## [22] "Existing_variation" "Multiallelic"wecare_nfe_variants.df[1:5,1:5]## SplitVarID SYMBOL TYPE CHROM POS
## Var000000002 Var000000002 LINC00115 SNP 1 762330
## Var000000008 Var000000008 SAMD11 SNP 1 871215
## Var000000009 Var000000009 SAMD11 SNP 1 871230
## Var000000012 Var000000012 SAMD11 INDEL 1 874778
## Var000000013 Var000000013 SAMD11 SNP 1 878664dim(wecare_nfe_kgen.df)## [1] 275516 9colnames(wecare_nfe_kgen.df)## [1] "SplitVarID" "kgen.AC" "kgen.AN" "kgen.AF" "kgen.AFR_AF"
## [6] "kgen.AMR_AF" "kgen.EAS_AF" "kgen.EUR_AF" "kgen.SAS_AF"wecare_nfe_kgen.df[1:5,1:5]## SplitVarID kgen.AC kgen.AN kgen.AF kgen.AFR_AF
## Var000000002 Var000000002 NA NA NA NA
## Var000000008 Var000000008 NA NA NA NA
## Var000000009 Var000000009 NA NA NA NA
## Var000000012 Var000000012 NA NA NA NA
## Var000000013 Var000000013 2 5008 0.000399361 0dim(wecare_nfe_exac.df)## [1] 275516 48colnames(wecare_nfe_exac.df)## [1] "SplitVarID" "exac_non_TCGA.AF"
## [3] "exac_non_TCGA.AC" "exac_non_TCGA.AN"
## [5] "exac_non_TCGA.AC_FEMALE" "exac_non_TCGA.AN_FEMALE"
## [7] "exac_non_TCGA.AC_MALE" "exac_non_TCGA.AN_MALE"
## [9] "exac_non_TCGA.AC_Adj" "exac_non_TCGA.AN_Adj"
## [11] "exac_non_TCGA.AC_Hom" "exac_non_TCGA.AC_Het"
## [13] "exac_non_TCGA.AC_Hemi" "exac_non_TCGA.AC_AFR"
## [15] "exac_non_TCGA.AN_AFR" "exac_non_TCGA.Hom_AFR"
## [17] "exac_non_TCGA.Het_AFR" "exac_non_TCGA.Hemi_AFR"
## [19] "exac_non_TCGA.AC_AMR" "exac_non_TCGA.AN_AMR"
## [21] "exac_non_TCGA.Hom_AMR" "exac_non_TCGA.Het_AMR"
## [23] "exac_non_TCGA.Hemi_AMR" "exac_non_TCGA.AC_EAS"
## [25] "exac_non_TCGA.AN_EAS" "exac_non_TCGA.Hom_EAS"
## [27] "exac_non_TCGA.Het_EAS" "exac_non_TCGA.Hemi_EAS"
## [29] "exac_non_TCGA.AC_FIN" "exac_non_TCGA.AN_FIN"
## [31] "exac_non_TCGA.Hom_FIN" "exac_non_TCGA.Het_FIN"
## [33] "exac_non_TCGA.Hemi_FIN" "exac_non_TCGA.AC_NFE"
## [35] "exac_non_TCGA.AN_NFE" "exac_non_TCGA.Hom_NFE"
## [37] "exac_non_TCGA.Het_NFE" "exac_non_TCGA.Hemi_NFE"
## [39] "exac_non_TCGA.AC_SAS" "exac_non_TCGA.AN_SAS"
## [41] "exac_non_TCGA.Hom_SAS" "exac_non_TCGA.Het_SAS"
## [43] "exac_non_TCGA.Hemi_SAS" "exac_non_TCGA.AC_OTH"
## [45] "exac_non_TCGA.AN_OTH" "exac_non_TCGA.Hom_OTH"
## [47] "exac_non_TCGA.Het_OTH" "exac_non_TCGA.Hemi_OTH"wecare_nfe_exac.df[1:5,1:5]## SplitVarID exac_non_TCGA.AF exac_non_TCGA.AC
## Var000000002 Var000000002 0.0120000 175
## Var000000008 Var000000008 NA NA
## Var000000009 Var000000009 NA NA
## Var000000012 Var000000012 NA NA
## Var000000013 Var000000013 0.0005838 62
## exac_non_TCGA.AN exac_non_TCGA.AC_FEMALE
## Var000000002 14012 59
## Var000000008 NA NA
## Var000000009 NA NA
## Var000000012 NA NA
## Var000000013 106198 17# Check consistency of colnames and rownames
sum(colnames(wecare_nfe_genotypes.mx) != rownames(wecare_nfe_phenotypes.df))## [1] 0sum(rownames(wecare_nfe_genotypes.mx) != rownames(wecare_nfe_variants.df))## [1] 0sum(rownames(wecare_nfe_genotypes.mx) != rownames(wecare_nfe_kgen.df))## [1] 0sum(rownames(wecare_nfe_genotypes.mx) != rownames(wecare_nfe_exac.df))## [1] 0function_to_calculate_eigenvectors
Implements procedure described by Price et al 2006 (PMID: 16862161)
normalise_and_calculate_eigenvectors.udf <- function(x) {
# --- Center and normalise variants (rows) --- #
# Center by mean
avg.rows <- apply(x, 1, mean, na.rm=TRUE)
x.c <- x - avg.rows
# Normalise by sqrt(p(1-p)) where p~"posterior estimate of unobserved allele frequency"
# This is motivated by the fact that genetic drift per generation is proportional to this normalisation value (Patterson 2006)
# Also this makes each column to have same variance
#
p.fnc <- function(x) (1 + sum(x, na.rm=TRUE)) / (2 + 2 * sum(!is.na(x)))
p <- apply(x, 1, p.fnc)
eaf <- sqrt(p*(1-p))
x.cn <- x.c/eaf
# Substitute NAs to zeros
0 -> x.cn[is.na(x)]
# --- Calculate eigenvectors of covariance matrix of cases --- #
cov.mx <- cov(x.cn)
eig <- eigen(cov.mx) # eigenvectors in columns
return(eig)
}make_wecare_only_subset_of_data
# Remove nfe cases
wecare_cases <- as.vector(wecare_nfe_phenotypes.df[wecare_nfe_phenotypes.df$cc!=-1,"wes_id"])
length(wecare_cases) # 480## [1] 480wecare_genotypes.mx <- wecare_nfe_genotypes.mx[,wecare_cases]
dim(wecare_genotypes.mx) # 275,516 x 480## [1] 275516 480wecare_genotypes.mx[1:5,1:5]## P1_A01 P1_A02 P1_A03 P1_A04 P1_A05
## Var000000002 0 0 0 0 0
## Var000000008 0 0 NA 0 NA
## Var000000009 0 NA NA 0 NA
## Var000000012 0 NA NA 0 0
## Var000000013 0 NA 0 0 0wecare_phenotypes.df <- wecare_nfe_phenotypes.df[wecare_cases,]
dim(wecare_phenotypes.df) # 480 x 28## [1] 480 28wecare_phenotypes.df[1:5,1:5]## wes_id gwas_id merged_id filter cc
## P1_A01 P1_A01 id203568 P1_A01_id203568 pass 1
## P1_A02 P1_A02 id357807 P1_A02_id357807 pass 1
## P1_A03 P1_A03 id325472 P1_A03_id325472 pass 1
## P1_A04 P1_A04 id304354 P1_A04_id304354 pass 1
## P1_A05 P1_A05 id222648 P1_A05_id222648 pass 1# Clean-up
rm(wecare_cases)remove_variants_with_uniform_genotypes_accross_all_wecare_samples
Remove 50,141 variants: 275,516 -> 225,375
# Check that there is no all-NA variants
non_NA_count.udf <- function(x){sum(!is.na(x))}
all_NA <- apply(wecare_genotypes.mx, 1, non_NA_count.udf) == 0
sum(all_NA) # 0## [1] 0# Function to detect uniform numeric vector
uniform_vector.udf <- function(x){
if(min(x, na.rm=TRUE) == max(x, na.rm=TRUE)){return(TRUE)} else {return(FALSE)}}
# Variants with uniform genotypes accross all samples
uniform_genotypes <- apply(wecare_genotypes.mx, 1, uniform_vector.udf)
summary(uniform_genotypes)## Mode FALSE TRUE NA's
## logical 225375 50141 0sum(uniform_genotypes) # 50,141## [1] 50141# Remove variants with uniform genotypes accross all samples
wecare_genotypes.mx <- wecare_genotypes.mx[!uniform_genotypes,]
dim(wecare_genotypes.mx) # 225375 480## [1] 225375 480wecare_genotypes.mx[1:5,1:5]## P1_A01 P1_A02 P1_A03 P1_A04 P1_A05
## Var000000002 0 0 0 0 0
## Var000000008 0 0 NA 0 NA
## Var000000009 0 NA NA 0 NA
## Var000000012 0 NA NA 0 0
## Var000000013 0 NA 0 0 0wecare_variants.df <- wecare_nfe_variants.df[!uniform_genotypes,]
dim(wecare_variants.df) # 225375 23## [1] 225375 23wecare_variants.df[1:5,1:5]## SplitVarID SYMBOL TYPE CHROM POS
## Var000000002 Var000000002 LINC00115 SNP 1 762330
## Var000000008 Var000000008 SAMD11 SNP 1 871215
## Var000000009 Var000000009 SAMD11 SNP 1 871230
## Var000000012 Var000000012 SAMD11 INDEL 1 874778
## Var000000013 Var000000013 SAMD11 SNP 1 878664wecare_kgen.df <- wecare_nfe_kgen.df[!uniform_genotypes,]
dim(wecare_kgen.df) # 225375 9## [1] 225375 9wecare_kgen.df[1:5,1:5]## SplitVarID kgen.AC kgen.AN kgen.AF kgen.AFR_AF
## Var000000002 Var000000002 NA NA NA NA
## Var000000008 Var000000008 NA NA NA NA
## Var000000009 Var000000009 NA NA NA NA
## Var000000012 Var000000012 NA NA NA NA
## Var000000013 Var000000013 2 5008 0.000399361 0wecare_exac.df <- wecare_nfe_exac.df[!uniform_genotypes,]
dim(wecare_exac.df) # 225375 48## [1] 225375 48wecare_exac.df[1:5,1:5]## SplitVarID exac_non_TCGA.AF exac_non_TCGA.AC
## Var000000002 Var000000002 0.0120000 175
## Var000000008 Var000000008 NA NA
## Var000000009 Var000000009 NA NA
## Var000000012 Var000000012 NA NA
## Var000000013 Var000000013 0.0005838 62
## exac_non_TCGA.AN exac_non_TCGA.AC_FEMALE
## Var000000002 14012 59
## Var000000008 NA NA
## Var000000009 NA NA
## Var000000012 NA NA
## Var000000013 106198 17# Clean-up
rm(non_NA_count.udf, all_NA, uniform_vector.udf, uniform_genotypes)calculate_and_plot_eigenvectors_wecare_all_variants
# --- Calculate eigenvectors --- #
wecare_eigen <- normalise_and_calculate_eigenvectors.udf(wecare_genotypes.mx)
wecare_all_variants_eigenvectors.df <- as.data.frame(wecare_eigen$vectors) # eigenvectors in columns
wecare_all_variants_eigenvalues <- wecare_eigen$values
# --- Prepare data for plotting --- #
# Prepare colour scale
colours <- c("UBC" = "BLUE", "CBC" = "RED")
userColourScale <- scale_colour_manual(values=colours)
# Prepare cases lables
cases_labels <- as.vector(wecare_phenotypes.df$cc)
"CBC" -> cases_labels[cases_labels==1]
"UBC" -> cases_labels[cases_labels==0]
# Prepare cases IDs
cases_IDs <- as.vector(wecare_phenotypes.df$wes_id)
# make the dataframe
data2plot.df <- cbind(cases_IDs, cases_labels, wecare_all_variants_eigenvectors.df[,1:3])
colnames(data2plot.df) <- c("wes_id", "group", "ev1", "ev2", "ev3")
# --- Plot eig1 vs eig2 --- #
g <- ggplot(data2plot.df, aes(ev1, ev2)) +
geom_point(aes(colour=group, fill=group, text = wes_id)) +
labs(title="wecare all variants<br>(225,375 x 480)", x ="eigenvector1", y = "eigenvector2") +
userColourScale## Warning: Ignoring unknown aesthetics: textggplotly(g)# --- Plot eig2 vs eig3 --- #
g <- ggplot(data2plot.df, aes(ev2, ev3)) +
geom_point(aes(colour=group, fill=group, text = wes_id)) +
labs(title="wecare all variants<br>(225,375 x 480)", x ="eigenvector2", y = "eigenvector3") +
userColourScale## Warning: Ignoring unknown aesthetics: textggplotly(g)# --- Clean-up --- #
rm(wecare_all_variants_eigenvectors.df, wecare_all_variants_eigenvalues, g, data2plot.df)export_wecare_all_variants_to_EIGENSTRAT_format
# --- make snp file --- #
# Extract data from variants table
wecare_all_variants_snp.df <- wecare_variants.df %>%
mutate(morgan = POS / 1000000) %>%
select(SplitVarID, CHROM, morgan, POS, REF, ALT)
# Recode CRHOM data
summary(wecare_all_variants_snp.df$CHROM)## 1 10 11 12 13 14 15 16 17 18 19 2
## 22787 9409 13267 11893 4130 7634 7668 9444 12300 3822 13376 16992
## 20 21 22 3 4 5 6 7 8 9 MT X
## 5406 2740 4940 13234 9060 10265 13081 10359 7728 9305 361 6173
## Y
## 1str(wecare_all_variants_snp.df)## 'data.frame': 225375 obs. of 6 variables:
## $ SplitVarID: Factor w/ 343824 levels "Var000000001",..: 2 8 9 12 13 20 21 23 24 25 ...
## $ CHROM : Factor w/ 25 levels "1","10","11",..: 1 1 1 1 1 1 1 1 1 1 ...
## $ morgan : num 0.762 0.871 0.871 0.875 0.879 ...
## $ POS : int 762330 871215 871230 874778 878664 880461 880483 880917 881627 881825 ...
## $ REF : Factor w/ 2142 levels "A","AAAAAAAAAAAAAAAAAAAAAAAG",..: 1044 539 539 1231 1044 539 1 1044 1044 539 ...
## $ ALT : Factor w/ 1297 levels "A","AAAAAAAAAAAAACT",..: 989 664 989 664 1 989 664 1 1 989 ...wecare_all_variants_snp.df$CHROM <- as.vector(wecare_all_variants_snp.df$CHROM)
str(wecare_all_variants_snp.df)## 'data.frame': 225375 obs. of 6 variables:
## $ SplitVarID: Factor w/ 343824 levels "Var000000001",..: 2 8 9 12 13 20 21 23 24 25 ...
## $ CHROM : chr "1" "1" "1" "1" ...
## $ morgan : num 0.762 0.871 0.871 0.875 0.879 ...
## $ POS : int 762330 871215 871230 874778 878664 880461 880483 880917 881627 881825 ...
## $ REF : Factor w/ 2142 levels "A","AAAAAAAAAAAAAAAAAAAAAAAG",..: 1044 539 539 1231 1044 539 1 1044 1044 539 ...
## $ ALT : Factor w/ 1297 levels "A","AAAAAAAAAAAAACT",..: 989 664 989 664 1 989 664 1 1 989 ..."23" -> wecare_all_variants_snp.df[wecare_all_variants_snp.df$CHROM == "X", "CHROM"]
"24" -> wecare_all_variants_snp.df[wecare_all_variants_snp.df$CHROM == "Y", "CHROM"]
"90" -> wecare_all_variants_snp.df[wecare_all_variants_snp.df$CHROM == "MT", "CHROM"]
wecare_all_variants_snp.df$CHROM <- as.factor(wecare_all_variants_snp.df$CHROM)
summary(wecare_all_variants_snp.df$CHROM)## 1 10 11 12 13 14 15 16 17 18 19 2
## 22787 9409 13267 11893 4130 7634 7668 9444 12300 3822 13376 16992
## 20 21 22 23 24 3 4 5 6 7 8 9
## 5406 2740 4940 6173 1 13234 9060 10265 13081 10359 7728 9305
## 90
## 361# Write file (tab-separated)
write.table(wecare_all_variants_snp.df,
paste(interim_data_folder, "wecare_all_variants.snp", sep="/"),
quote=FALSE, sep="\t",
row.names=FALSE, col.names=FALSE)
# --- make geno file --- #
# Get data from genotypes matrix
wecare_all_variants_geno.mx <- wecare_genotypes.mx
# Recode NA
9 -> wecare_all_variants_geno.mx[is.na(wecare_all_variants_geno.mx)] # NA is coded as 9
# Write file (no delimiters!)
write.table(wecare_all_variants_geno.mx,
paste(interim_data_folder, "wecare_all_variants.geno", sep="/"),
quote=FALSE, sep="",
row.names=FALSE, col.names=FALSE)
# --- make ind file --- #
# Samples column
samples <- as.vector(wecare_phenotypes.df$wes_id)
# Gender column
gender <- rep("F", length(samples)) # all females
# Population/Group column
group <- as.vector(wecare_phenotypes.df$cc)
"UBC" -> group[group == 0]
"CBC" -> group[group == 1]
# Get together
wecare_ind.mx <- cbind(samples, gender, group)
# Write file (tab-separated)
write.table(wecare_ind.mx,
paste(interim_data_folder, "wecare.ind", sep="/"),
quote=FALSE, sep="\t",
row.names=FALSE, col.names=FALSE)
rm(wecare_all_variants_snp.df, wecare_all_variants_geno.mx, wecare_ind.mx, samples, gender, group)calculate_and_plot_eigenvectors_wecare_common_variants
# --- Calculate AFs --- #
ac_wecare_cln <- apply(wecare_genotypes.mx, 1, sum, na.rm=TRUE)
get_allele_number.udf <- function(x){2*sum(!is.na(x))}
an_wecare_cln <- apply(wecare_genotypes.mx, 1, get_allele_number.udf)
af_wecare_cln <- ac_wecare_cln/an_wecare_cln
# Ceck AFs
# (note that uniform variants were excluded)
ac_wecare_cln[1:10]## Var000000002 Var000000008 Var000000009 Var000000012 Var000000013
## 4 3 1 37 1
## Var000000020 Var000000021 Var000000023 Var000000024 Var000000025
## 1 1 1 581 1an_wecare_cln[1:10]## Var000000002 Var000000008 Var000000009 Var000000012 Var000000013
## 950 834 806 776 820
## Var000000020 Var000000021 Var000000023 Var000000024 Var000000025
## 956 958 958 902 928af_wecare_cln[1:10]## Var000000002 Var000000008 Var000000009 Var000000012 Var000000013
## 0.004210526 0.003597122 0.001240695 0.047680412 0.001219512
## Var000000020 Var000000021 Var000000023 Var000000024 Var000000025
## 0.001046025 0.001043841 0.001043841 0.644124169 0.001077586min(ac_wecare_cln)## [1] 1min(an_wecare_cln)## [1] 688min(af_wecare_cln)## [1] 0.001041667max(ac_wecare_cln)## [1] 959max(an_wecare_cln)## [1] 960max(af_wecare_cln)## [1] 0.9989583# Add updated AFs to wecare_variants.df
wecare_variants.df <- cbind(wecare_variants.df,
ac_wecare_cln, an_wecare_cln, af_wecare_cln)
# --- Exclude rare variants --- #
# Note exclusion on both sides: high- and low- AFs
# Low AFs remove rare variants with common allele in reference genome
# Hight AFs remove rare variants with common allele in reference genome
wecare_common_vars <- af_wecare_cln > 0.05 & af_wecare_cln < 0.95
sum(wecare_common_vars) # 44,517## [1] 44517min(af_wecare_cln[wecare_common_vars])## [1] 0.05010438max(af_wecare_cln[wecare_common_vars])## [1] 0.9498956common_wecare_genotypes.mx <- wecare_genotypes.mx[wecare_common_vars,]
dim(common_wecare_genotypes.mx)## [1] 44517 480common_wecare_genotypes.mx[1:5,1:5]## P1_A01 P1_A02 P1_A03 P1_A04 P1_A05
## Var000000024 2 1 NA 1 2
## Var000000027 0 NA NA 1 NA
## Var000000037 0 NA NA 0 NA
## Var000000054 2 2 NA 2 NA
## Var000000058 2 2 2 2 2common_wecare_variants.df <- wecare_variants.df[wecare_common_vars,]
dim(common_wecare_variants.df)## [1] 44517 26common_wecare_variants.df[1:5,1:5]## SplitVarID SYMBOL TYPE CHROM POS
## Var000000024 Var000000024 NOC2L SNP 1 881627
## Var000000027 Var000000027 NOC2L SNP 1 881918
## Var000000037 Var000000037 NOC2L SNP 1 889238
## Var000000054 Var000000054 KLHL17 SNP 1 897325
## Var000000058 Var000000058 KLHL17 SNP 1 897564common_wecare_kgen.df <- wecare_kgen.df[wecare_common_vars,]
dim(common_wecare_kgen.df)## [1] 44517 9common_wecare_kgen.df[1:5,1:5]## SplitVarID kgen.AC kgen.AN kgen.AF kgen.AFR_AF
## Var000000024 Var000000024 2213 5008 0.4418930 0.0643
## Var000000027 Var000000027 147 5008 0.0293530 0.0038
## Var000000037 Var000000037 283 5008 0.0565096 0.0197
## Var000000054 Var000000054 4303 5008 0.8592250 0.6959
## Var000000058 Var000000058 4507 5008 0.8999600 0.8298common_wecare_exac.df <- wecare_exac.df[wecare_common_vars,]
dim(common_wecare_exac.df)## [1] 44517 48common_wecare_exac.df[1:5,1:5]## SplitVarID exac_non_TCGA.AF exac_non_TCGA.AC
## Var000000024 Var000000024 0.562 59637
## Var000000027 Var000000027 0.045 4735
## Var000000037 Var000000037 NA NA
## Var000000054 Var000000054 NA NA
## Var000000058 Var000000058 0.898 70551
## exac_non_TCGA.AN exac_non_TCGA.AC_FEMALE
## Var000000024 106210 24874
## Var000000027 106208 1867
## Var000000037 NA NA
## Var000000054 NA NA
## Var000000058 78540 4650# --- Calculate eigenvectors --- #
common_wecare_eigen <- normalise_and_calculate_eigenvectors.udf(common_wecare_genotypes.mx)
wecare_common_variants_eigenvectors.df <- as.data.frame(common_wecare_eigen$vectors) # eigenvectors in columns
wecare_common_variants_eigenvalues <- common_wecare_eigen$values
# --- Prepare data for plotting --- #
data2plot.df <- cbind(cases_IDs, cases_labels, wecare_common_variants_eigenvectors.df[,1:3])
colnames(data2plot.df) <- c("wes_id", "group", "ev1", "ev2", "ev3")
# --- Plot eig1 vs eig2 --- #
g <- ggplot(data2plot.df, aes(-ev1, ev2)) +
geom_point(aes(colour=group, fill=group, text = wes_id)) +
labs(title="wecare common variants<br>(44,517 x 480)", x ="-eigenvector1", y = "eigenvector2") +
userColourScale## Warning: Ignoring unknown aesthetics: textggplotly(g)# --- Plot eig2 vs eig3 --- #
g <- ggplot(data2plot.df, aes(ev2, ev3)) +
geom_point(aes(colour=group, fill=group, text = wes_id)) +
labs(title="wecare common variants<br>(44,517 x 480)", x ="eigenvector2", y = "eigenvector3") +
userColourScale## Warning: Ignoring unknown aesthetics: textggplotly(g)# --- Clean-up --- #
rm(wecare_common_variants_eigenvectors.df, wecare_common_variants_eigenvalues, g, data2plot.df,
cases_labels, cases_IDs, colours, userColourScale, wecare_common_vars,
ac_wecare_cln, an_wecare_cln, af_wecare_cln,
get_allele_number.udf, normalise_and_calculate_eigenvectors.udf)export_wecare_common_variants_to_EIGENSTRAT_format
# --- make snp file --- #
# Extract data from variants table
wecare_common_variants_snp.df <- common_wecare_variants.df %>%
mutate(morgan = POS / 1000000) %>%
select(SplitVarID, CHROM, morgan, POS, REF, ALT)
# Recode CRHOM data
summary(wecare_common_variants_snp.df$CHROM)## 1 10 11 12 13 14 15 16 17 18 19 2 20 21 22
## 4352 1983 2783 2342 816 1587 1401 1682 2417 788 2984 3200 1118 594 1008
## 3 4 5 6 7 8 9 MT X Y
## 2485 1796 2097 2888 2083 1471 1821 16 804 1str(wecare_common_variants_snp.df)## 'data.frame': 44517 obs. of 6 variables:
## $ SplitVarID: Factor w/ 343824 levels "Var000000001",..: 24 27 37 54 58 62 75 99 109 139 ...
## $ CHROM : Factor w/ 25 levels "1","10","11",..: 1 1 1 1 1 1 1 1 1 1 ...
## $ morgan : num 0.882 0.882 0.889 0.897 0.898 ...
## $ POS : int 881627 881918 889238 897325 897564 897738 900505 909309 911916 948846 ...
## $ REF : Factor w/ 2142 levels "A","AAAAAAAAAAAAAAAAAAAAAAAG",..: 1044 1044 1044 1044 1575 539 1044 1575 539 1575 ...
## $ ALT : Factor w/ 1297 levels "A","AAAAAAAAAAAAACT",..: 1 1 1 323 323 989 323 323 989 990 ...wecare_common_variants_snp.df$CHROM <- as.vector(wecare_common_variants_snp.df$CHROM)
str(wecare_common_variants_snp.df)## 'data.frame': 44517 obs. of 6 variables:
## $ SplitVarID: Factor w/ 343824 levels "Var000000001",..: 24 27 37 54 58 62 75 99 109 139 ...
## $ CHROM : chr "1" "1" "1" "1" ...
## $ morgan : num 0.882 0.882 0.889 0.897 0.898 ...
## $ POS : int 881627 881918 889238 897325 897564 897738 900505 909309 911916 948846 ...
## $ REF : Factor w/ 2142 levels "A","AAAAAAAAAAAAAAAAAAAAAAAG",..: 1044 1044 1044 1044 1575 539 1044 1575 539 1575 ...
## $ ALT : Factor w/ 1297 levels "A","AAAAAAAAAAAAACT",..: 1 1 1 323 323 989 323 323 989 990 ..."23" -> wecare_common_variants_snp.df[wecare_common_variants_snp.df$CHROM == "X", "CHROM"]
"24" -> wecare_common_variants_snp.df[wecare_common_variants_snp.df$CHROM == "Y", "CHROM"]
"90" -> wecare_common_variants_snp.df[wecare_common_variants_snp.df$CHROM == "MT", "CHROM"]
wecare_common_variants_snp.df$CHROM <- as.factor(wecare_common_variants_snp.df$CHROM)
summary(wecare_common_variants_snp.df$CHROM)## 1 10 11 12 13 14 15 16 17 18 19 2 20 21 22
## 4352 1983 2783 2342 816 1587 1401 1682 2417 788 2984 3200 1118 594 1008
## 23 24 3 4 5 6 7 8 9 90
## 804 1 2485 1796 2097 2888 2083 1471 1821 16# Write file (tab-separated)
write.table(wecare_common_variants_snp.df,
paste(interim_data_folder, "wecare_common_variants.snp", sep="/"),
quote=FALSE, sep="\t",
row.names=FALSE, col.names=FALSE)
# --- make geno file --- #
# Get data from genotypes matrix
wecare_common_variants_geno.mx <- common_wecare_genotypes.mx
# Recode NA
9 -> wecare_common_variants_geno.mx[is.na(wecare_common_variants_geno.mx)] # NA is coded as 9
# Write file (no delimiters)
write.table(wecare_common_variants_geno.mx,
paste(interim_data_folder, "wecare_common_variants.geno", sep="/"),
quote=FALSE, sep="",
row.names=FALSE, col.names=FALSE)
# --- make ind file --- #
# has been made for wecare all variants
rm(wecare_common_variants_snp.df, wecare_common_variants_geno.mx)compare_eigenvalues_and_eigenvectors_in_all_and_common_variants
# --- Compare eigenvalues --- #
eval_all <- wecare_eigen$values
eval_common <- common_wecare_eigen$values
plot(eval_all, main="Wecare eigenvalues (all variants)")
plot(eval_common, main="Wecare igenvalues (common variants)")
plot(eval_all,eval_common, main="Wecare eigenvalues (all vs common variants)")
# --- Compare eigenvectors --- #
# Gather data
ev1_all <- wecare_eigen$vectors[,1]
ev1_common <- common_wecare_eigen$vectors[,1]
ev2_all <- wecare_eigen$vectors[,2]
ev2_common <- common_wecare_eigen$vectors[,2]
ev3_all <- wecare_eigen$vectors[,3]
ev3_common <- common_wecare_eigen$vectors[,3]
data2plot.df <- as.data.frame(cbind(ev1_all, ev2_all, ev3_all, ev1_common, ev2_common, ev3_common))
# Calculate correlations
cor.test(ev1_all, ev1_common) # -0.482982, p-value = 2.2e-16##
## Pearson's product-moment correlation
##
## data: ev1_all and ev1_common
## t = -12.059, df = 478, p-value < 2.2e-16
## alternative hypothesis: true correlation is not equal to 0
## 95 percent confidence interval:
## -0.5487611 -0.4112591
## sample estimates:
## cor
## -0.482982cor.test(ev2_all, ev2_common) # -0.2196824, p-value = 1.174e-06##
## Pearson's product-moment correlation
##
## data: ev2_all and ev2_common
## t = -4.9232, df = 478, p-value = 1.174e-06
## alternative hypothesis: true correlation is not equal to 0
## 95 percent confidence interval:
## -0.3032210 -0.1327928
## sample estimates:
## cor
## -0.2196824cor.test(ev3_all, ev3_common) # -0.06442268, p-value = 0.1588##
## Pearson's product-moment correlation
##
## data: ev3_all and ev3_common
## t = -1.4114, df = 478, p-value = 0.1588
## alternative hypothesis: true correlation is not equal to 0
## 95 percent confidence interval:
## -0.15304072 0.02522321
## sample estimates:
## cor
## -0.06442268# Common sence check (these eigenvectors should be orthogonal...)
cor.test(ev1_all, ev2_all) # -3.530534e-16, p-value = 1##
## Pearson's product-moment correlation
##
## data: ev1_all and ev2_all
## t = -2.1423e-14, df = 478, p-value = 1
## alternative hypothesis: true correlation is not equal to 0
## 95 percent confidence interval:
## -0.08950045 0.08950045
## sample estimates:
## cor
## -9.798722e-16cor.test(ev1_common, ev2_common) # -6.391521e-16, p-value = 1##
## Pearson's product-moment correlation
##
## data: ev1_common and ev2_common
## t = 4.9748e-15, df = 478, p-value = 1
## alternative hypothesis: true correlation is not equal to 0
## 95 percent confidence interval:
## -0.08950045 0.08950045
## sample estimates:
## cor
## 2.275435e-16# Make plots
g <- ggplot(data2plot.df, aes(ev1_all, ev1_common)) +
geom_point() +
labs(title="Wecare eigenvector 1<br>all vs common variants (p=2e-16)")
ggplotly(g)g <- ggplot(data2plot.df, aes(ev2_all, ev2_common)) +
geom_point() +
labs(title="Wecare eigenvector 2<br>all vs common variants (p=1e-06)")
ggplotly(g)g <- ggplot(data2plot.df, aes(ev3_all, ev3_common)) +
geom_point() +
labs(title="Wecare eigenvector 3<br>all vs common variants (p=0.16)")
ggplotly(g)# Clean-up
rm(eval_all, eval_common, ev1_all, ev2_all, ev3_all, ev1_common, ev2_common, ev3_common, g, data2plot.df)data_summary
ls()## [1] "common_wecare_eigen" "common_wecare_exac.df"
## [3] "common_wecare_genotypes.mx" "common_wecare_kgen.df"
## [5] "common_wecare_variants.df" "interim_data_folder"
## [7] "wecare_eigen" "wecare_exac.df"
## [9] "wecare_genotypes.mx" "wecare_kgen.df"
## [11] "wecare_nfe_exac.df" "wecare_nfe_genotypes.mx"
## [13] "wecare_nfe_kgen.df" "wecare_nfe_phenotypes.df"
## [15] "wecare_nfe_variants.df" "wecare_phenotypes.df"
## [17] "wecare_variants.df"# --- wecare nfe --- #
dim(wecare_nfe_genotypes.mx)## [1] 275516 678class(wecare_nfe_genotypes.mx)## [1] "matrix"wecare_nfe_genotypes.mx[1:5,1:5]## HG00097 HG00099 HG00100 HG00102 HG00106
## Var000000002 0 0 NA NA 0
## Var000000008 0 NA 0 0 0
## Var000000009 0 0 0 0 0
## Var000000012 0 0 NA 0 0
## Var000000013 0 0 NA 0 0dim(wecare_nfe_phenotypes.df)## [1] 678 28str(wecare_nfe_phenotypes.df)## 'data.frame': 678 obs. of 28 variables:
## $ wes_id : chr "HG00097" "HG00099" "HG00100" "HG00102" ...
## $ gwas_id : chr NA NA NA NA ...
## $ merged_id : chr NA NA NA NA ...
## $ filter : chr "pass" "pass" "pass" "pass" ...
## $ cc : num -1 -1 -1 -1 -1 -1 -1 -1 -1 -1 ...
## $ setno : int NA NA NA NA NA NA NA NA NA NA ...
## $ family_history: int NA NA NA NA NA NA NA NA NA NA ...
## $ age_dx : int NA NA NA NA NA NA NA NA NA NA ...
## $ age_ref : num NA NA NA NA NA NA NA NA NA NA ...
## $ rstime : num NA NA NA NA NA NA NA NA NA NA ...
## $ eig1_gwas : num NA NA NA NA NA NA NA NA NA NA ...
## $ eig2_gwas : num NA NA NA NA NA NA NA NA NA NA ...
## $ eig3_gwas : num NA NA NA NA NA NA NA NA NA NA ...
## $ stage : num NA NA NA NA NA NA NA NA NA NA ...
## $ er : num NA NA NA NA NA NA NA NA NA NA ...
## $ pr : num NA NA NA NA NA NA NA NA NA NA ...
## $ hist_cat : chr NA NA NA NA ...
## $ hormone : num NA NA NA NA NA NA NA NA NA NA ...
## $ chemo_cat : chr NA NA NA NA ...
## $ br_xray : int NA NA NA NA NA NA NA NA NA NA ...
## $ br_xray_dose : num NA NA NA NA NA NA NA NA NA NA ...
## $ age_menarche : num NA NA NA NA NA NA NA NA NA NA ...
## $ age_1st_ftp : num NA NA NA NA NA NA NA NA NA NA ...
## $ age_menopause : num NA NA NA NA NA NA NA NA NA NA ...
## $ num_preg : num NA NA NA NA NA NA NA NA NA NA ...
## $ bmi_age18 : num NA NA NA NA NA NA NA NA NA NA ...
## $ bmi_dx : num NA NA NA NA NA NA NA NA NA NA ...
## $ bmi_ref : num NA NA NA NA NA NA NA NA NA NA ...wecare_nfe_phenotypes.df[1:5,1:5]## wes_id gwas_id merged_id filter cc
## HG00097 HG00097 <NA> <NA> pass -1
## HG00099 HG00099 <NA> <NA> pass -1
## HG00100 HG00100 <NA> <NA> pass -1
## HG00102 HG00102 <NA> <NA> pass -1
## HG00106 HG00106 <NA> <NA> pass -1dim(wecare_nfe_variants.df)## [1] 275516 23colnames(wecare_nfe_variants.df)## [1] "SplitVarID" "SYMBOL" "TYPE"
## [4] "CHROM" "POS" "REF"
## [7] "ALT" "AC" "AF"
## [10] "AN" "Consequence" "SIFT_call"
## [13] "SIFT_score" "PolyPhen_call" "PolyPhen_score"
## [16] "CLIN_SIG" "cDNA_position" "CDS_position"
## [19] "Codons" "Protein_position" "Amino_acids"
## [22] "Existing_variation" "Multiallelic"wecare_nfe_variants.df[1:5,1:5]## SplitVarID SYMBOL TYPE CHROM POS
## Var000000002 Var000000002 LINC00115 SNP 1 762330
## Var000000008 Var000000008 SAMD11 SNP 1 871215
## Var000000009 Var000000009 SAMD11 SNP 1 871230
## Var000000012 Var000000012 SAMD11 INDEL 1 874778
## Var000000013 Var000000013 SAMD11 SNP 1 878664dim(wecare_nfe_kgen.df)## [1] 275516 9colnames(wecare_nfe_kgen.df)## [1] "SplitVarID" "kgen.AC" "kgen.AN" "kgen.AF" "kgen.AFR_AF"
## [6] "kgen.AMR_AF" "kgen.EAS_AF" "kgen.EUR_AF" "kgen.SAS_AF"wecare_nfe_kgen.df[1:5,1:5]## SplitVarID kgen.AC kgen.AN kgen.AF kgen.AFR_AF
## Var000000002 Var000000002 NA NA NA NA
## Var000000008 Var000000008 NA NA NA NA
## Var000000009 Var000000009 NA NA NA NA
## Var000000012 Var000000012 NA NA NA NA
## Var000000013 Var000000013 2 5008 0.000399361 0dim(wecare_nfe_exac.df)## [1] 275516 48colnames(wecare_nfe_exac.df)## [1] "SplitVarID" "exac_non_TCGA.AF"
## [3] "exac_non_TCGA.AC" "exac_non_TCGA.AN"
## [5] "exac_non_TCGA.AC_FEMALE" "exac_non_TCGA.AN_FEMALE"
## [7] "exac_non_TCGA.AC_MALE" "exac_non_TCGA.AN_MALE"
## [9] "exac_non_TCGA.AC_Adj" "exac_non_TCGA.AN_Adj"
## [11] "exac_non_TCGA.AC_Hom" "exac_non_TCGA.AC_Het"
## [13] "exac_non_TCGA.AC_Hemi" "exac_non_TCGA.AC_AFR"
## [15] "exac_non_TCGA.AN_AFR" "exac_non_TCGA.Hom_AFR"
## [17] "exac_non_TCGA.Het_AFR" "exac_non_TCGA.Hemi_AFR"
## [19] "exac_non_TCGA.AC_AMR" "exac_non_TCGA.AN_AMR"
## [21] "exac_non_TCGA.Hom_AMR" "exac_non_TCGA.Het_AMR"
## [23] "exac_non_TCGA.Hemi_AMR" "exac_non_TCGA.AC_EAS"
## [25] "exac_non_TCGA.AN_EAS" "exac_non_TCGA.Hom_EAS"
## [27] "exac_non_TCGA.Het_EAS" "exac_non_TCGA.Hemi_EAS"
## [29] "exac_non_TCGA.AC_FIN" "exac_non_TCGA.AN_FIN"
## [31] "exac_non_TCGA.Hom_FIN" "exac_non_TCGA.Het_FIN"
## [33] "exac_non_TCGA.Hemi_FIN" "exac_non_TCGA.AC_NFE"
## [35] "exac_non_TCGA.AN_NFE" "exac_non_TCGA.Hom_NFE"
## [37] "exac_non_TCGA.Het_NFE" "exac_non_TCGA.Hemi_NFE"
## [39] "exac_non_TCGA.AC_SAS" "exac_non_TCGA.AN_SAS"
## [41] "exac_non_TCGA.Hom_SAS" "exac_non_TCGA.Het_SAS"
## [43] "exac_non_TCGA.Hemi_SAS" "exac_non_TCGA.AC_OTH"
## [45] "exac_non_TCGA.AN_OTH" "exac_non_TCGA.Hom_OTH"
## [47] "exac_non_TCGA.Het_OTH" "exac_non_TCGA.Hemi_OTH"wecare_nfe_exac.df[1:5,1:5]## SplitVarID exac_non_TCGA.AF exac_non_TCGA.AC
## Var000000002 Var000000002 0.0120000 175
## Var000000008 Var000000008 NA NA
## Var000000009 Var000000009 NA NA
## Var000000012 Var000000012 NA NA
## Var000000013 Var000000013 0.0005838 62
## exac_non_TCGA.AN exac_non_TCGA.AC_FEMALE
## Var000000002 14012 59
## Var000000008 NA NA
## Var000000009 NA NA
## Var000000012 NA NA
## Var000000013 106198 17sum(colnames(wecare_nfe_genotypes.mx) != rownames(wecare_nfe_phenotypes.df))## [1] 0sum(rownames(wecare_nfe_genotypes.mx) != rownames(wecare_nfe_variants.df))## [1] 0sum(rownames(wecare_nfe_genotypes.mx) != rownames(wecare_nfe_kgen.df))## [1] 0sum(rownames(wecare_nfe_genotypes.mx) != rownames(wecare_nfe_exac.df))## [1] 0# --- wecare only all variants --- #
dim(wecare_genotypes.mx)## [1] 225375 480class(wecare_genotypes.mx)## [1] "matrix"wecare_genotypes.mx[1:5,1:5]## P1_A01 P1_A02 P1_A03 P1_A04 P1_A05
## Var000000002 0 0 0 0 0
## Var000000008 0 0 NA 0 NA
## Var000000009 0 NA NA 0 NA
## Var000000012 0 NA NA 0 0
## Var000000013 0 NA 0 0 0dim(wecare_phenotypes.df)## [1] 480 28str(wecare_phenotypes.df)## 'data.frame': 480 obs. of 28 variables:
## $ wes_id : chr "P1_A01" "P1_A02" "P1_A03" "P1_A04" ...
## $ gwas_id : chr "id203568" "id357807" "id325472" "id304354" ...
## $ merged_id : chr "P1_A01_id203568" "P1_A02_id357807" "P1_A03_id325472" "P1_A04_id304354" ...
## $ filter : chr "pass" "pass" "pass" "pass" ...
## $ cc : num 1 1 1 1 1 1 0 1 1 0 ...
## $ setno : int 203568 357807 325472 304354 222648 244843 276284 297810 250898 226974 ...
## $ family_history: int 1 0 1 1 1 1 1 1 1 0 ...
## $ age_dx : int 49 35 32 33 44 28 28 38 35 36 ...
## $ age_ref : num 58 36 41 34 49 28 32 44 35 38 ...
## $ rstime : num 10.17 1.83 9.75 1.59 5.66 ...
## $ eig1_gwas : num -0.00389 -0.00379 -0.01011 -0.01288 -0.01086 ...
## $ eig2_gwas : num 0.00266 0.00246 -0.0001 0.00595 0.01157 ...
## $ eig3_gwas : num 0.06803 0.05055 -0.00603 0.00747 0.00144 ...
## $ stage : num 1 2 2 1 1 1 2 1 2 1 ...
## $ er : num NA 0 0 0 NA 1 1 1 1 0 ...
## $ pr : num NA 0 0 NA NA 1 NA 1 0 0 ...
## $ hist_cat : chr "lobular" "ductal" "medullary" "ductal" ...
## $ hormone : num 0 0 0 0 1 0 0 0 0 0 ...
## $ chemo_cat : chr "no" "CMF" "Oth" "no" ...
## $ br_xray : int 1 1 0 0 1 0 0 0 1 1 ...
## $ br_xray_dose : num 1.6 0.83 0 0 0.77 0 0 0 1.1 0.83 ...
## $ age_menarche : num 9 13 10 12 10 13 12 11 11 NA ...
## $ age_1st_ftp : num 30 0 26 0 17 0 25 28 27 18 ...
## $ age_menopause : num -1 -1 -1 -1 -1 -1 -1 -1 -1 -1 ...
## $ num_preg : num 1 0 1 0 1 0 1 1 1 1 ...
## $ bmi_age18 : num 20.8 22.5 23.6 18.6 19.9 ...
## $ bmi_dx : num 25.8 22.9 28.3 17.8 26.6 ...
## $ bmi_ref : num 33.3 22.9 33.1 17.8 29.8 ...wecare_phenotypes.df[1:5,1:5]## wes_id gwas_id merged_id filter cc
## P1_A01 P1_A01 id203568 P1_A01_id203568 pass 1
## P1_A02 P1_A02 id357807 P1_A02_id357807 pass 1
## P1_A03 P1_A03 id325472 P1_A03_id325472 pass 1
## P1_A04 P1_A04 id304354 P1_A04_id304354 pass 1
## P1_A05 P1_A05 id222648 P1_A05_id222648 pass 1dim(wecare_variants.df)## [1] 225375 26colnames(wecare_variants.df)## [1] "SplitVarID" "SYMBOL" "TYPE"
## [4] "CHROM" "POS" "REF"
## [7] "ALT" "AC" "AF"
## [10] "AN" "Consequence" "SIFT_call"
## [13] "SIFT_score" "PolyPhen_call" "PolyPhen_score"
## [16] "CLIN_SIG" "cDNA_position" "CDS_position"
## [19] "Codons" "Protein_position" "Amino_acids"
## [22] "Existing_variation" "Multiallelic" "ac_wecare_cln"
## [25] "an_wecare_cln" "af_wecare_cln"wecare_variants.df[1:5,1:5]## SplitVarID SYMBOL TYPE CHROM POS
## Var000000002 Var000000002 LINC00115 SNP 1 762330
## Var000000008 Var000000008 SAMD11 SNP 1 871215
## Var000000009 Var000000009 SAMD11 SNP 1 871230
## Var000000012 Var000000012 SAMD11 INDEL 1 874778
## Var000000013 Var000000013 SAMD11 SNP 1 878664dim(wecare_kgen.df)## [1] 225375 9colnames(wecare_kgen.df)## [1] "SplitVarID" "kgen.AC" "kgen.AN" "kgen.AF" "kgen.AFR_AF"
## [6] "kgen.AMR_AF" "kgen.EAS_AF" "kgen.EUR_AF" "kgen.SAS_AF"wecare_kgen.df[1:5,1:5]## SplitVarID kgen.AC kgen.AN kgen.AF kgen.AFR_AF
## Var000000002 Var000000002 NA NA NA NA
## Var000000008 Var000000008 NA NA NA NA
## Var000000009 Var000000009 NA NA NA NA
## Var000000012 Var000000012 NA NA NA NA
## Var000000013 Var000000013 2 5008 0.000399361 0dim(wecare_exac.df)## [1] 225375 48colnames(wecare_exac.df)## [1] "SplitVarID" "exac_non_TCGA.AF"
## [3] "exac_non_TCGA.AC" "exac_non_TCGA.AN"
## [5] "exac_non_TCGA.AC_FEMALE" "exac_non_TCGA.AN_FEMALE"
## [7] "exac_non_TCGA.AC_MALE" "exac_non_TCGA.AN_MALE"
## [9] "exac_non_TCGA.AC_Adj" "exac_non_TCGA.AN_Adj"
## [11] "exac_non_TCGA.AC_Hom" "exac_non_TCGA.AC_Het"
## [13] "exac_non_TCGA.AC_Hemi" "exac_non_TCGA.AC_AFR"
## [15] "exac_non_TCGA.AN_AFR" "exac_non_TCGA.Hom_AFR"
## [17] "exac_non_TCGA.Het_AFR" "exac_non_TCGA.Hemi_AFR"
## [19] "exac_non_TCGA.AC_AMR" "exac_non_TCGA.AN_AMR"
## [21] "exac_non_TCGA.Hom_AMR" "exac_non_TCGA.Het_AMR"
## [23] "exac_non_TCGA.Hemi_AMR" "exac_non_TCGA.AC_EAS"
## [25] "exac_non_TCGA.AN_EAS" "exac_non_TCGA.Hom_EAS"
## [27] "exac_non_TCGA.Het_EAS" "exac_non_TCGA.Hemi_EAS"
## [29] "exac_non_TCGA.AC_FIN" "exac_non_TCGA.AN_FIN"
## [31] "exac_non_TCGA.Hom_FIN" "exac_non_TCGA.Het_FIN"
## [33] "exac_non_TCGA.Hemi_FIN" "exac_non_TCGA.AC_NFE"
## [35] "exac_non_TCGA.AN_NFE" "exac_non_TCGA.Hom_NFE"
## [37] "exac_non_TCGA.Het_NFE" "exac_non_TCGA.Hemi_NFE"
## [39] "exac_non_TCGA.AC_SAS" "exac_non_TCGA.AN_SAS"
## [41] "exac_non_TCGA.Hom_SAS" "exac_non_TCGA.Het_SAS"
## [43] "exac_non_TCGA.Hemi_SAS" "exac_non_TCGA.AC_OTH"
## [45] "exac_non_TCGA.AN_OTH" "exac_non_TCGA.Hom_OTH"
## [47] "exac_non_TCGA.Het_OTH" "exac_non_TCGA.Hemi_OTH"wecare_exac.df[1:5,1:5]## SplitVarID exac_non_TCGA.AF exac_non_TCGA.AC
## Var000000002 Var000000002 0.0120000 175
## Var000000008 Var000000008 NA NA
## Var000000009 Var000000009 NA NA
## Var000000012 Var000000012 NA NA
## Var000000013 Var000000013 0.0005838 62
## exac_non_TCGA.AN exac_non_TCGA.AC_FEMALE
## Var000000002 14012 59
## Var000000008 NA NA
## Var000000009 NA NA
## Var000000012 NA NA
## Var000000013 106198 17sum(colnames(wecare_genotypes.mx) != rownames(wecare_phenotypes.df))## [1] 0sum(rownames(wecare_genotypes.mx) != rownames(wecare_variants.df))## [1] 0sum(rownames(wecare_genotypes.mx) != rownames(wecare_kgen.df))## [1] 0sum(rownames(wecare_genotypes.mx) != rownames(wecare_exac.df))## [1] 0# --- wecare only common variants --- #
dim(common_wecare_genotypes.mx)## [1] 44517 480class(common_wecare_genotypes.mx)## [1] "matrix"common_wecare_genotypes.mx[1:5,1:5]## P1_A01 P1_A02 P1_A03 P1_A04 P1_A05
## Var000000024 2 1 NA 1 2
## Var000000027 0 NA NA 1 NA
## Var000000037 0 NA NA 0 NA
## Var000000054 2 2 NA 2 NA
## Var000000058 2 2 2 2 2dim(wecare_phenotypes.df) # same as in rare## [1] 480 28str(wecare_phenotypes.df)## 'data.frame': 480 obs. of 28 variables:
## $ wes_id : chr "P1_A01" "P1_A02" "P1_A03" "P1_A04" ...
## $ gwas_id : chr "id203568" "id357807" "id325472" "id304354" ...
## $ merged_id : chr "P1_A01_id203568" "P1_A02_id357807" "P1_A03_id325472" "P1_A04_id304354" ...
## $ filter : chr "pass" "pass" "pass" "pass" ...
## $ cc : num 1 1 1 1 1 1 0 1 1 0 ...
## $ setno : int 203568 357807 325472 304354 222648 244843 276284 297810 250898 226974 ...
## $ family_history: int 1 0 1 1 1 1 1 1 1 0 ...
## $ age_dx : int 49 35 32 33 44 28 28 38 35 36 ...
## $ age_ref : num 58 36 41 34 49 28 32 44 35 38 ...
## $ rstime : num 10.17 1.83 9.75 1.59 5.66 ...
## $ eig1_gwas : num -0.00389 -0.00379 -0.01011 -0.01288 -0.01086 ...
## $ eig2_gwas : num 0.00266 0.00246 -0.0001 0.00595 0.01157 ...
## $ eig3_gwas : num 0.06803 0.05055 -0.00603 0.00747 0.00144 ...
## $ stage : num 1 2 2 1 1 1 2 1 2 1 ...
## $ er : num NA 0 0 0 NA 1 1 1 1 0 ...
## $ pr : num NA 0 0 NA NA 1 NA 1 0 0 ...
## $ hist_cat : chr "lobular" "ductal" "medullary" "ductal" ...
## $ hormone : num 0 0 0 0 1 0 0 0 0 0 ...
## $ chemo_cat : chr "no" "CMF" "Oth" "no" ...
## $ br_xray : int 1 1 0 0 1 0 0 0 1 1 ...
## $ br_xray_dose : num 1.6 0.83 0 0 0.77 0 0 0 1.1 0.83 ...
## $ age_menarche : num 9 13 10 12 10 13 12 11 11 NA ...
## $ age_1st_ftp : num 30 0 26 0 17 0 25 28 27 18 ...
## $ age_menopause : num -1 -1 -1 -1 -1 -1 -1 -1 -1 -1 ...
## $ num_preg : num 1 0 1 0 1 0 1 1 1 1 ...
## $ bmi_age18 : num 20.8 22.5 23.6 18.6 19.9 ...
## $ bmi_dx : num 25.8 22.9 28.3 17.8 26.6 ...
## $ bmi_ref : num 33.3 22.9 33.1 17.8 29.8 ...wecare_phenotypes.df[1:5,1:5]## wes_id gwas_id merged_id filter cc
## P1_A01 P1_A01 id203568 P1_A01_id203568 pass 1
## P1_A02 P1_A02 id357807 P1_A02_id357807 pass 1
## P1_A03 P1_A03 id325472 P1_A03_id325472 pass 1
## P1_A04 P1_A04 id304354 P1_A04_id304354 pass 1
## P1_A05 P1_A05 id222648 P1_A05_id222648 pass 1dim(common_wecare_variants.df)## [1] 44517 26colnames(common_wecare_variants.df)## [1] "SplitVarID" "SYMBOL" "TYPE"
## [4] "CHROM" "POS" "REF"
## [7] "ALT" "AC" "AF"
## [10] "AN" "Consequence" "SIFT_call"
## [13] "SIFT_score" "PolyPhen_call" "PolyPhen_score"
## [16] "CLIN_SIG" "cDNA_position" "CDS_position"
## [19] "Codons" "Protein_position" "Amino_acids"
## [22] "Existing_variation" "Multiallelic" "ac_wecare_cln"
## [25] "an_wecare_cln" "af_wecare_cln"common_wecare_variants.df[1:5,1:5]## SplitVarID SYMBOL TYPE CHROM POS
## Var000000024 Var000000024 NOC2L SNP 1 881627
## Var000000027 Var000000027 NOC2L SNP 1 881918
## Var000000037 Var000000037 NOC2L SNP 1 889238
## Var000000054 Var000000054 KLHL17 SNP 1 897325
## Var000000058 Var000000058 KLHL17 SNP 1 897564dim(common_wecare_kgen.df)## [1] 44517 9colnames(common_wecare_kgen.df)## [1] "SplitVarID" "kgen.AC" "kgen.AN" "kgen.AF" "kgen.AFR_AF"
## [6] "kgen.AMR_AF" "kgen.EAS_AF" "kgen.EUR_AF" "kgen.SAS_AF"common_wecare_kgen.df[1:5,1:5]## SplitVarID kgen.AC kgen.AN kgen.AF kgen.AFR_AF
## Var000000024 Var000000024 2213 5008 0.4418930 0.0643
## Var000000027 Var000000027 147 5008 0.0293530 0.0038
## Var000000037 Var000000037 283 5008 0.0565096 0.0197
## Var000000054 Var000000054 4303 5008 0.8592250 0.6959
## Var000000058 Var000000058 4507 5008 0.8999600 0.8298dim(common_wecare_exac.df)## [1] 44517 48colnames(common_wecare_exac.df)## [1] "SplitVarID" "exac_non_TCGA.AF"
## [3] "exac_non_TCGA.AC" "exac_non_TCGA.AN"
## [5] "exac_non_TCGA.AC_FEMALE" "exac_non_TCGA.AN_FEMALE"
## [7] "exac_non_TCGA.AC_MALE" "exac_non_TCGA.AN_MALE"
## [9] "exac_non_TCGA.AC_Adj" "exac_non_TCGA.AN_Adj"
## [11] "exac_non_TCGA.AC_Hom" "exac_non_TCGA.AC_Het"
## [13] "exac_non_TCGA.AC_Hemi" "exac_non_TCGA.AC_AFR"
## [15] "exac_non_TCGA.AN_AFR" "exac_non_TCGA.Hom_AFR"
## [17] "exac_non_TCGA.Het_AFR" "exac_non_TCGA.Hemi_AFR"
## [19] "exac_non_TCGA.AC_AMR" "exac_non_TCGA.AN_AMR"
## [21] "exac_non_TCGA.Hom_AMR" "exac_non_TCGA.Het_AMR"
## [23] "exac_non_TCGA.Hemi_AMR" "exac_non_TCGA.AC_EAS"
## [25] "exac_non_TCGA.AN_EAS" "exac_non_TCGA.Hom_EAS"
## [27] "exac_non_TCGA.Het_EAS" "exac_non_TCGA.Hemi_EAS"
## [29] "exac_non_TCGA.AC_FIN" "exac_non_TCGA.AN_FIN"
## [31] "exac_non_TCGA.Hom_FIN" "exac_non_TCGA.Het_FIN"
## [33] "exac_non_TCGA.Hemi_FIN" "exac_non_TCGA.AC_NFE"
## [35] "exac_non_TCGA.AN_NFE" "exac_non_TCGA.Hom_NFE"
## [37] "exac_non_TCGA.Het_NFE" "exac_non_TCGA.Hemi_NFE"
## [39] "exac_non_TCGA.AC_SAS" "exac_non_TCGA.AN_SAS"
## [41] "exac_non_TCGA.Hom_SAS" "exac_non_TCGA.Het_SAS"
## [43] "exac_non_TCGA.Hemi_SAS" "exac_non_TCGA.AC_OTH"
## [45] "exac_non_TCGA.AN_OTH" "exac_non_TCGA.Hom_OTH"
## [47] "exac_non_TCGA.Het_OTH" "exac_non_TCGA.Hemi_OTH"common_wecare_exac.df[1:5,1:5]## SplitVarID exac_non_TCGA.AF exac_non_TCGA.AC
## Var000000024 Var000000024 0.562 59637
## Var000000027 Var000000027 0.045 4735
## Var000000037 Var000000037 NA NA
## Var000000054 Var000000054 NA NA
## Var000000058 Var000000058 0.898 70551
## exac_non_TCGA.AN exac_non_TCGA.AC_FEMALE
## Var000000024 106210 24874
## Var000000027 106208 1867
## Var000000037 NA NA
## Var000000054 NA NA
## Var000000058 78540 4650sum(colnames(common_wecare_genotypes.mx) != rownames(wecare_phenotypes.df))## [1] 0sum(rownames(common_wecare_genotypes.mx) != rownames(common_wecare_variants.df))## [1] 0sum(rownames(common_wecare_genotypes.mx) != rownames(common_wecare_kgen.df))## [1] 0sum(rownames(common_wecare_genotypes.mx) != rownames(common_wecare_exac.df))## [1] 0save_data
save.image(paste(interim_data_folder, "r05_calculate_egenvectors_wecare_only_jan2017.RData", sep="/"))final_section
ls()## [1] "common_wecare_eigen" "common_wecare_exac.df"
## [3] "common_wecare_genotypes.mx" "common_wecare_kgen.df"
## [5] "common_wecare_variants.df" "interim_data_folder"
## [7] "wecare_eigen" "wecare_exac.df"
## [9] "wecare_genotypes.mx" "wecare_kgen.df"
## [11] "wecare_nfe_exac.df" "wecare_nfe_genotypes.mx"
## [13] "wecare_nfe_kgen.df" "wecare_nfe_phenotypes.df"
## [15] "wecare_nfe_variants.df" "wecare_phenotypes.df"
## [17] "wecare_variants.df"sessionInfo()## R version 3.2.3 (2015-12-10)
## Platform: x86_64-pc-linux-gnu (64-bit)
## Running under: Scientific Linux release 6.8 (Carbon)
##
## locale:
## [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
## [3] LC_TIME=en_US.UTF-8 LC_COLLATE=en_US.UTF-8
## [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
## [7] LC_PAPER=en_US.UTF-8 LC_NAME=C
## [9] LC_ADDRESS=C LC_TELEPHONE=C
## [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
##
## attached base packages:
## [1] stats graphics grDevices utils datasets methods base
##
## other attached packages:
## [1] plotly_4.5.6 ggplot2_2.2.1 dplyr_0.5.0
##
## loaded via a namespace (and not attached):
## [1] Rcpp_0.12.6 knitr_1.13 magrittr_1.5
## [4] munsell_0.4.3 viridisLite_0.1.3 colorspace_1.2-6
## [7] R6_2.1.2 httr_1.2.1 stringr_1.0.0
## [10] plyr_1.8.4 tools_3.2.3 grid_3.2.3
## [13] gtable_0.2.0 DBI_0.5 htmltools_0.3.5
## [16] yaml_2.1.13 lazyeval_0.2.0 assertthat_0.1
## [19] digest_0.6.10 tibble_1.1 tidyr_0.5.1
## [22] purrr_0.2.2 formatR_1.4 base64enc_0.1-3
## [25] htmlwidgets_0.8 evaluate_0.9 rmarkdown_1.0
## [28] labeling_0.3 stringi_1.1.1 scales_0.4.1
## [31] jsonlite_1.0Sys.time()## [1] "2017-02-09 16:08:20 GMT"